Publications by authors named "Bora Ergin"

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Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect.
Aynur Küçükçongar Yavaş, Sümeyra Zeynep Özbey, Bora Ergin, Yasemin Ünal, Berrak Bilginer Gürbüz

Mol Syndromol· October 2025

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De Novo Cloning and Functional Characterization of a Mechanosensitive Piezo-Like Ion Channel in the Crayfish.
Bora Ergin, Berk Saglam, Kaan Arslan, Nazlı Coskun Beyatli, Zihni Ekim Taskiran

Cell Physiol Biochem· July 2023

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Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux.
Gülsüm Kayman Kürekçi, Ecem Kural Mangit, Cansu Koyunlar, Seyda Unsal, Berk Saglam, Bora Ergin

Sci Rep· April 2021

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Cloning of a putative sodium/calcium exchanger gene in the crayfish.
Bora Ergin, Nuhan Purali

Invert Neurosci· July 2018

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